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eNauka >  Rezultati >  3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: case report of a child with rare HMGCL gene variants
Naziv: 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: case report of a child with rare HMGCL gene variants
Autori: Bjelica, Milena; Stojadinovic, Aleksandra; Knezevic-Pogancev, Marija F; Koprivsek, Katarina M; Sass, Jorn Oliver; Gruenert, Sarah C; Wuensche, Falko; Yamamoto, Raina
Godina: 2025
Publikacija: JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
ISSN: 0334-018X Journal of Pediatric Endocrinology and Metabolism Pretraži identifikator
Tip rezultata: Naučni članak
DOI: 10.1515/jpem-2025-0156
WoS-ID: 001508184600001
Scopus-ID: 2-s2.0-105008342601
URI: https://enauka.gov.rs/handle/123456789/986672
Projekat: MVZ Dr. Eberhard & Partner Dortmund [514177501, 528562393-FIP26, 538669957]
Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)
Izvor metapodataka: (Preuzeto iz Nasi u WoS)
M-kategorija: 
22M22 - Međunarodni časopis kategorije M22

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